Transcript #00025496 (NM_001277115.1, DNAH11 gene)

Transcript name dynein, axonemal, heavy chain 11
Gene name DNAH11 (dynein, axonemal, heavy chain 11)
Chromosome 7
Transcript - NCBI ID NM_001277115.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_001264044.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 2020-02-16 12:46:52 +01:00 (CET)
Date last edited N/A


Variants

432 entries on 5 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-/. - c.54C>T r.(?) p.(Thr18=)
-/. - c.100G>T r.(?) p.(Glu34Ter)
-/. - c.100G>T r.(?) p.(Glu34Ter)
-/. - c.100_101delinsTT r.(?) p.(Glu34Leu)
-/. - c.101A>T r.(?) p.(Glu34Val)
+/. - c.163C>T r.(?) p.(Gln55*)
+/. - c.165del r.(?) p.(Asp56Thrfs*13)
?/. - c.188G>C r.(?) p.(Gly63Ala)
+?/. - c.384del r.(?) p.(Phe128Leufs*12)
-/. - c.421G>T r.(?) p.(Asp141Tyr)
?/. - c.423C>A r.(?) p.(Asp141Glu)
?/. - c.434T>A r.(?) p.(Val145Glu)
?/. - c.470G>A r.(?) p.(Gly157Glu)
?/. - c.495+3A>T r.spl? p.?
+/. - c.503del r.(?) p.(Val168Glyfs*25)
?/. - c.576A>G r.(?) p.(Ile192Met)
-/. - c.576A>G r.(?) p.(Ile192Met)
-?/. - c.640A>G r.(?) p.(Ile214Val)
?/. - c.640A>G r.(?) p.(Ile214Val)
?/. - c.661A>T r.(?) p.(Met221Leu)
-?/. - c.661A>T r.(?) p.(Met221Leu)
-?/. - c.661A>T r.(?) p.(Met221Leu)
?/. - c.661A>T r.(?) p.(Met221Leu)
-?/. - c.695C>T r.(?) p.(Pro232Leu)
-?/. - c.695C>T r.(?) p.(Pro232Leu)
-/. - c.705C>T r.(?) p.(Asn235=)
-/. - c.705C>T r.(?) p.(Asn235=)
?/. - c.773T>C r.(?) p.(Ile258Thr)
+/. - c.793_794insCAGCT r.(?) p.(Arg265Profs*5)
-?/. - c.939C>T r.(?) p.(Ser313=)
-?/. - c.939C>T r.(?) p.(Ser313=)
-/. - c.971C>T r.(?) p.(Ala324Val)
?/. - c.991G>A r.(?) p.(Glu331Lys)
-/. - c.1065A>G r.(?) p.(Pro355=)
-?/. - c.1072C>T r.(?) p.(Arg358Cys)
?/. - c.1148G>A r.(?) p.(Arg383Gln)
-?/. - c.1194+57C>T r.(=) p.(=)
-?/. - c.1199C>T r.(?) p.(Thr400Ile)
-?/. - c.1199C>T r.(?) p.(Thr400Ile)
-/. - c.1199C>T r.(?) p.(Thr400Ile)
-/. - c.1199C>T r.(?) p.(Thr400Ile)
?/. - c.1232G>A r.(?) p.(Gly411Glu)
?/. - c.1241A>G r.(?) p.(Glu414Gly)
+/. - c.1320dup r.(?) p.(Leu441Ilefs*25)
-/. - c.1397A>C r.(?) p.(Lys466Thr)
-/. - c.1426-9T>C r.(=) p.(=)
-/. - c.1426-9T>C r.(=) p.(=)
-?/. - c.1426-4A>G r.spl? p.?
?/. - c.1478G>A r.(?) p.(Gly493Asp)
?/. - c.1586C>G r.(?) p.(Thr529Ser)
-?/. - c.1586C>G r.(?) p.(Thr529Ser)
?/. - c.1593G>T r.(?) p.(Met531Ile)
-?/. - c.1702G>A r.(?) p.(Ala568Thr)
-/. - c.1702G>A r.(?) p.(Ala568Thr)
-?/. - c.1702G>A r.(?) p.(Ala568Thr)
-/. - c.1702G>A r.(?) p.(Ala568Thr)
+?/. - c.1846C>T r.(?) p.(Gln616Ter)
-/. - c.1916A>G r.(?) p.(Gln639Arg)
-/. - c.1956C>T r.(?) p.(Phe652=)
-/. - c.1956C>T r.(?) p.(Phe652=)
-/. - c.1961C>G r.(?) p.(Ser654Cys)
?/. - c.1997C>G r.(?) p.(Ala666Gly)
+/. - c.2068dup r.(?) p.(Trp690Leufs*4)
+/. - c.2152_2153del r.(?) p.(Val718Glnfs*3)
?/. - c.2176G>T r.(?) p.(Ala726Ser)
-/. - c.2275-15G>T r.(=) p.(=)
-?/. - c.2379C>T r.(?) p.(Asp793=)
-/. - c.2454A>G r.(?) p.(Ala818=)
-/. - c.2454A>G r.(?) p.(Ala818=)
?/. - c.2542G>A r.(?) p.(Val848Met)
?/. - c.2542G>A r.(?) p.(Val848Met)
-?/. - c.2570G>A r.(?) p.(Arg857Gln)
-?/. - c.2587T>C r.(?) p.(Leu863=)
+?/. - c.2712G>A r.(?) p.(Trp904*)
-?/. - c.2750A>T r.(?) p.(Glu917Val)
-?/. - c.2772G>A r.(?) p.(Met924Ile)
?/. - c.2772G>A r.(?) p.(Met924Ile)
-?/. - c.2783A>T r.(?) p.(Asp928Val)
-?/. - c.2803G>A r.(?) p.(Glu935Lys)
?/. - c.2824C>A r.(?) p.(Pro942Thr)
-/. - c.2835A>G r.(?) p.(Gln945=)
-/. - c.2835A>G r.(?) p.(Gln945=)
+/. - c.2849del r.(?) p.(Leu950Cysfs*12)
-?/. - c.2887A>G r.(?) p.(Arg963Gly)
+?/. - c.2966G>A r.(?) p.(Arg989Gln)
?/. - c.3040C>G r.(?) p.(Gln1014Glu)
-?/. - c.3045G>T r.(?) p.(Glu1015Asp)
+?/. - c.3045G>T r.(?) p.(Glu1015Asp)
-/. - c.3068T>C r.(?) p.(Val1023Ala)
-/. - c.3112A>G r.(?) p.(Thr1038Ala)
-/. - c.3112A>G r.(?) p.(Thr1038Ala)
?/. - c.3174T>A r.(?) p.(=)
?/. - c.3236T>C r.(?) p.(Leu1079Pro)
-?/. - c.3237T>C r.(?) p.(Leu1079=)
-/. - c.3256-10C>G r.(=) p.(=)
-?/. - c.3263T>C r.(?) p.(Ile1088Thr)
?/. - c.3356G>A r.(?) p.(Ser1119Asn)
?/. - c.3356G>A r.(?) p.(Ser1119Asn)
-?/. - c.3412T>C r.(?) p.(Phe1138Leu)
?/. - c.3466G>A r.(?) p.(Gly1156Arg)
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